Obtaining a patient’s consent is not the same as having a patient sign a consent form. While a written, countersigned document provides important evidence if consent is disputed in court, in order for ...

Informed consent is one of the most important aspects of conducting ethical research with human participants. Respecting the autonomy of research participants, the investigator must provide complete ...

The healthcare landscape is undergoing a significant transformation, with health information exchanges (HIEs) and health data utilities (HDUs) playing a pivotal role in facilitating the secure ...

Informed consent is one of the primary requirements of research involving human participants. It is important to remember that informed consent is an ongoing process, not a document or single event.

The Nuremberg Code (1947) and the Declaration of Helsinki (1978) are credited as the origins of informed consent in clinical research. Participants' informed consent is both a legal and ethical ...

Obtaining valid consent is a fundamental part of providing quality care and a key ethical and legal requirement in medicine. Issues around consent can, however, trip up even the most experienced ...

Informed consent is more than just a form; it is a process that actively involves the participant. It is an "ongoing exchange of information between the investigator and [participant]" per the OHRP.

Obtaining informed consent is more than getting a signature on a form. Informed consent is one of the primary ethical considerations underlying research with human subjects. ALL human subject research ...

When we talk about consent, we often frame it as a pretty simple concept. In a sense, it is — it’s a plain truth that you need to respect a partner’s “no,” no matter what. But the underlying process ...

It is the policy of Western Michigan University that all research involving human subjects will be reviewed by the Institutional Review Board. The involvement of human subjects in research is not ...